A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024130



Internal ID21933473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1427049..1427198hg38UCSC Ensembl
chr17:1330343..1330492hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627097
Samples
Known GenesCRK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024130
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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